Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000400766 |
Resumo: | The chemical investigation of ethyl acetate extract from Paepalanthus planifolius capitula resulted in the identification of 1H-naphtho[2,3-c]pyran-1-one,9-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-10-hydroxy-7-methoxy-3-methyl, semi-vioxanthin 9-O-β-D-glucopyranoside, toralactone-9-O-β-D-glucopyranoside, paepalantine-9-O-β-D-glucopyranoside, semi-vioxanthin, 1H-naphtho[2,3-c]pyran-1-one,3,4-dihydro-9,10-dihydroxy-5,7-dimethoxy-3-methyl, vioxanthin and paepalantine dimer, and also the isolation and identification of a new naphthopyranone dimer named planifoliusin A. The chemical structures of two compounds were elucidated by performing spectroscopic 1D and 2D nuclear magnetic resonance (NMR) experiments and spectrometric HRMS (high-resolution mass spectrometry) analysis. Other six naphthopyranone dimers were proposed by MS fragmentation patterns. The minimum inhibitory concentration (MIC) values for vioxanthin (7.8 µg mL-1), planifoliusin A (15.6 µg mL-1) and the ethyl acetate extract (31.2 µg mL-1) showed antimicrobial activity against Staphylococcus aureus (ATCC 25923). |
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Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human PathogensPaepalanthus planifoliusnaphthopyranoneantimicrobial activityThe chemical investigation of ethyl acetate extract from Paepalanthus planifolius capitula resulted in the identification of 1H-naphtho[2,3-c]pyran-1-one,9-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-10-hydroxy-7-methoxy-3-methyl, semi-vioxanthin 9-O-β-D-glucopyranoside, toralactone-9-O-β-D-glucopyranoside, paepalantine-9-O-β-D-glucopyranoside, semi-vioxanthin, 1H-naphtho[2,3-c]pyran-1-one,3,4-dihydro-9,10-dihydroxy-5,7-dimethoxy-3-methyl, vioxanthin and paepalantine dimer, and also the isolation and identification of a new naphthopyranone dimer named planifoliusin A. The chemical structures of two compounds were elucidated by performing spectroscopic 1D and 2D nuclear magnetic resonance (NMR) experiments and spectrometric HRMS (high-resolution mass spectrometry) analysis. Other six naphthopyranone dimers were proposed by MS fragmentation patterns. The minimum inhibitory concentration (MIC) values for vioxanthin (7.8 µg mL-1), planifoliusin A (15.6 µg mL-1) and the ethyl acetate extract (31.2 µg mL-1) showed antimicrobial activity against Staphylococcus aureus (ATCC 25923).Sociedade Brasileira de Química2018-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000400766Journal of the Brazilian Chemical Society v.29 n.4 2018reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20170199info:eu-repo/semantics/openAccessAmorim,Marcelo R. deHilário,FelipeSano,Paulo T.Bauab,Tais M.Santos,Lourdes C. doseng2018-03-12T00:00:00Zoai:scielo:S0103-50532018000400766Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2018-03-12T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens |
title |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens |
spellingShingle |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens Amorim,Marcelo R. de Paepalanthus planifolius naphthopyranone antimicrobial activity |
title_short |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens |
title_full |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens |
title_fullStr |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens |
title_full_unstemmed |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens |
title_sort |
Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens |
author |
Amorim,Marcelo R. de |
author_facet |
Amorim,Marcelo R. de Hilário,Felipe Sano,Paulo T. Bauab,Tais M. Santos,Lourdes C. dos |
author_role |
author |
author2 |
Hilário,Felipe Sano,Paulo T. Bauab,Tais M. Santos,Lourdes C. dos |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Amorim,Marcelo R. de Hilário,Felipe Sano,Paulo T. Bauab,Tais M. Santos,Lourdes C. dos |
dc.subject.por.fl_str_mv |
Paepalanthus planifolius naphthopyranone antimicrobial activity |
topic |
Paepalanthus planifolius naphthopyranone antimicrobial activity |
description |
The chemical investigation of ethyl acetate extract from Paepalanthus planifolius capitula resulted in the identification of 1H-naphtho[2,3-c]pyran-1-one,9-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-10-hydroxy-7-methoxy-3-methyl, semi-vioxanthin 9-O-β-D-glucopyranoside, toralactone-9-O-β-D-glucopyranoside, paepalantine-9-O-β-D-glucopyranoside, semi-vioxanthin, 1H-naphtho[2,3-c]pyran-1-one,3,4-dihydro-9,10-dihydroxy-5,7-dimethoxy-3-methyl, vioxanthin and paepalantine dimer, and also the isolation and identification of a new naphthopyranone dimer named planifoliusin A. The chemical structures of two compounds were elucidated by performing spectroscopic 1D and 2D nuclear magnetic resonance (NMR) experiments and spectrometric HRMS (high-resolution mass spectrometry) analysis. Other six naphthopyranone dimers were proposed by MS fragmentation patterns. The minimum inhibitory concentration (MIC) values for vioxanthin (7.8 µg mL-1), planifoliusin A (15.6 µg mL-1) and the ethyl acetate extract (31.2 µg mL-1) showed antimicrobial activity against Staphylococcus aureus (ATCC 25923). |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-04-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000400766 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000400766 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.21577/0103-5053.20170199 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.29 n.4 2018 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
_version_ |
1750318180485562368 |